A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5882688



Internal ID9023499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53712892..53716966hg38UCSC Ensembl
Outerchr20:53712733..53717165hg38UCSC Ensembl
Innerchr20:52329431..52333505hg19UCSC Ensembl
Outerchr20:52329272..52333704hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384433
hg194433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663190
Supporting Variants
SamplesHG00650
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5882688
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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